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Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation

G

Gachon University Gil Medical Center

Status

Enrolling

Conditions

Postoperative Pain

Treatments

Procedure: Intravenous fentanyl patient control device
Procedure: Erector Spinae Plane Block

Study type

Interventional

Funder types

Other

Identifiers

NCT04238780
ESPlapaAR

Details and patient eligibility

About

The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

Full description

.The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

Enrollment

60 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged between 20 and 70 years, with an American Society of Anesthesiologists physical status of 1 or 2, who were scheduled for laparoscopic colorectal operation

Exclusion criteria

  • sensitivity to local anesthetic, bleeding disorders , receiving anticoagulant, body mass index (BMI) over 35/kg/m2 spine or chest wall deformity pregnancy tolerance to opioid analgesics inability to use patient-controlled analgesia (PCA)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

ESP( Erector Spinae Plane Block)
Active Comparator group
Description:
After induction parturient in the ESPB underwent bilateral ESPB at the level of T7 using a linear ultrasound (US) transducer. Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.
Treatment:
Procedure: Erector Spinae Plane Block
Procedure: Intravenous fentanyl patient control device
control group
Active Comparator group
Description:
No regional anesthesia technique will be applied to the control group. Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.
Treatment:
Procedure: Intravenous fentanyl patient control device

Trial contacts and locations

1

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Central trial contact

jungju choi, nd,phd

Data sourced from clinicaltrials.gov

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